Device 2 of 2.Reference mfr.Report: 3006705815-2017-07307.It was reported the patient experienced weakness post-op, but the symptoms improved prior to the patient leaving the facility.The physician attributed this to the lidocaine used during the implant.On (b)(6) 2017, the patient reported feeling pain and lower extremity weakness and stated she planned to go to the er to have the leads explanted.As a result, the patient underwent explant for both trial leads.The pain and lower extremity weakness resolved after explant.
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